VACTERL association: Difference between revisions
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{{Infobox medical condition | |||
| name = VACTERL association | |||
| image = [[File:VACTERL.JPG|left|thumb|VACTERL association]] | |||
| caption = Diagram showing the features of VACTERL association | |||
| synonyms = VATER association | |||
| pronounce = | |||
| specialty = [[Medical genetics]] | |||
| symptoms = Vertebral anomalies, anal atresia, cardiac defects, tracheoesophageal fistula, renal anomalies, limb abnormalities | |||
| onset = Congenital | |||
| duration = Lifelong | |||
| causes = Unknown, possibly genetic and environmental factors | |||
| risks = | |||
| diagnosis = Clinical evaluation, imaging studies | |||
| differential = [[CHARGE syndrome]], [[Fanconi anemia]], [[Townes-Brocks syndrome]] | |||
| prevention = None | |||
| treatment = Surgical correction of anomalies, supportive care | |||
| medication = | |||
| prognosis = Variable, depends on severity and combination of anomalies | |||
| frequency = Rare | |||
| deaths = | |||
}} | |||
{{Short description|A non-random association of birth defects}} | {{Short description|A non-random association of birth defects}} | ||
'''VACTERL association''' is a non-random association of birth defects that affects multiple anatomical systems. The acronym VACTERL stands for: | '''VACTERL association''' is a non-random association of birth defects that affects multiple anatomical systems. The acronym VACTERL stands for: | ||
| Line 7: | Line 29: | ||
* '''R'''enal anomalies | * '''R'''enal anomalies | ||
* '''L'''imb abnormalities | * '''L'''imb abnormalities | ||
Individuals diagnosed with VACTERL association typically present with at least three of these congenital malformations. The exact cause of VACTERL association is not well understood, but it is believed to result from disruptions in embryonic development. | Individuals diagnosed with VACTERL association typically present with at least three of these congenital malformations. The exact cause of VACTERL association is not well understood, but it is believed to result from disruptions in embryonic development. | ||
==Clinical Features== | ==Clinical Features== | ||
===Vertebral Anomalies=== | ===Vertebral Anomalies=== | ||
Vertebral anomalies are present in approximately 60-80% of individuals with VACTERL association. These may include [[hemivertebrae]], [[vertebral fusion]], or [[scoliosis]]. | Vertebral anomalies are present in approximately 60-80% of individuals with VACTERL association. These may include [[hemivertebrae]], [[vertebral fusion]], or [[scoliosis]]. | ||
===Anal Atresia=== | ===Anal Atresia=== | ||
Anal atresia, also known as [[imperforate anus]], occurs in about 55-90% of cases. This condition requires surgical intervention shortly after birth to create a functional anal opening. | Anal atresia, also known as [[imperforate anus]], occurs in about 55-90% of cases. This condition requires surgical intervention shortly after birth to create a functional anal opening. | ||
===Cardiac Defects=== | ===Cardiac Defects=== | ||
Cardiac defects are found in 40-80% of individuals with VACTERL association. Common heart defects include [[ventricular septal defect]] (VSD), [[atrial septal defect]] (ASD), and [[tetralogy of Fallot]]. | Cardiac defects are found in 40-80% of individuals with VACTERL association. Common heart defects include [[ventricular septal defect]] (VSD), [[atrial septal defect]] (ASD), and [[tetralogy of Fallot]]. | ||
===Tracheo-Esophageal Fistula=== | ===Tracheo-Esophageal Fistula=== | ||
Tracheo-esophageal fistula (TEF) is present in approximately 50-80% of cases. This condition involves an abnormal connection between the trachea and esophagus, often accompanied by [[esophageal atresia]]. | Tracheo-esophageal fistula (TEF) is present in approximately 50-80% of cases. This condition involves an abnormal connection between the trachea and esophagus, often accompanied by [[esophageal atresia]]. | ||
===Renal Anomalies=== | ===Renal Anomalies=== | ||
Renal anomalies occur in 50-80% of individuals and may include [[renal agenesis]], [[horseshoe kidney]], or [[hydronephrosis]]. | Renal anomalies occur in 50-80% of individuals and may include [[renal agenesis]], [[horseshoe kidney]], or [[hydronephrosis]]. | ||
===Limb Abnormalities=== | ===Limb Abnormalities=== | ||
Limb abnormalities are present in 40-50% of cases. These may include [[radial aplasia]], [[polydactyly]], or [[syndactyly]]. | Limb abnormalities are present in 40-50% of cases. These may include [[radial aplasia]], [[polydactyly]], or [[syndactyly]]. | ||
==Diagnosis== | ==Diagnosis== | ||
Diagnosis of VACTERL association is primarily clinical, based on the presence of at least three of the characteristic anomalies. Prenatal diagnosis may be possible through [[ultrasound]] and other imaging techniques, but many cases are identified after birth. | Diagnosis of VACTERL association is primarily clinical, based on the presence of at least three of the characteristic anomalies. Prenatal diagnosis may be possible through [[ultrasound]] and other imaging techniques, but many cases are identified after birth. | ||
==Management== | ==Management== | ||
Management of VACTERL association is multidisciplinary, involving pediatricians, surgeons, cardiologists, and other specialists. Treatment is tailored to the specific anomalies present in each individual and may include surgical correction of defects, supportive care, and ongoing monitoring for complications. | Management of VACTERL association is multidisciplinary, involving pediatricians, surgeons, cardiologists, and other specialists. Treatment is tailored to the specific anomalies present in each individual and may include surgical correction of defects, supportive care, and ongoing monitoring for complications. | ||
==Prognosis== | ==Prognosis== | ||
The prognosis for individuals with VACTERL association varies depending on the severity and combination of anomalies. With appropriate medical and surgical management, many individuals can lead healthy lives, although they may require ongoing medical care. | The prognosis for individuals with VACTERL association varies depending on the severity and combination of anomalies. With appropriate medical and surgical management, many individuals can lead healthy lives, although they may require ongoing medical care. | ||
==See also== | |||
== | |||
* [[Congenital disorder]] | * [[Congenital disorder]] | ||
* [[Esophageal atresia]] | * [[Esophageal atresia]] | ||
* [[Congenital heart defect]] | * [[Congenital heart defect]] | ||
* [[Syndrome]] | * [[Syndrome]] | ||
[[Category:Congenital disorders]] | [[Category:Congenital disorders]] | ||
[[Category:Rare diseases]] | [[Category:Rare diseases]] | ||
Latest revision as of 15:34, 8 April 2025
Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC
| VACTERL association | |
|---|---|
 | |
| Synonyms | VATER association |
| Pronounce | |
| Specialty | Medical genetics |
| Symptoms | Vertebral anomalies, anal atresia, cardiac defects, tracheoesophageal fistula, renal anomalies, limb abnormalities |
| Complications | N/A |
| Onset | Congenital |
| Duration | Lifelong |
| Types | N/A |
| Causes | Unknown, possibly genetic and environmental factors |
| Risks | |
| Diagnosis | Clinical evaluation, imaging studies |
| Differential diagnosis | CHARGE syndrome, Fanconi anemia, Townes-Brocks syndrome |
| Prevention | None |
| Treatment | Surgical correction of anomalies, supportive care |
| Medication | |
| Prognosis | Variable, depends on severity and combination of anomalies |
| Frequency | Rare |
| Deaths | |
A non-random association of birth defects
VACTERL association is a non-random association of birth defects that affects multiple anatomical systems. The acronym VACTERL stands for:
- Vertebral anomalies
- Anal atresia
- Cardiac defects
- Tracheo-Esophageal fistula
- Renal anomalies
- Limb abnormalities
Individuals diagnosed with VACTERL association typically present with at least three of these congenital malformations. The exact cause of VACTERL association is not well understood, but it is believed to result from disruptions in embryonic development.
Clinical Features[edit]
Vertebral Anomalies[edit]
Vertebral anomalies are present in approximately 60-80% of individuals with VACTERL association. These may include hemivertebrae, vertebral fusion, or scoliosis.
Anal Atresia[edit]
Anal atresia, also known as imperforate anus, occurs in about 55-90% of cases. This condition requires surgical intervention shortly after birth to create a functional anal opening.
Cardiac Defects[edit]
Cardiac defects are found in 40-80% of individuals with VACTERL association. Common heart defects include ventricular septal defect (VSD), atrial septal defect (ASD), and tetralogy of Fallot.
Tracheo-Esophageal Fistula[edit]
Tracheo-esophageal fistula (TEF) is present in approximately 50-80% of cases. This condition involves an abnormal connection between the trachea and esophagus, often accompanied by esophageal atresia.
Renal Anomalies[edit]
Renal anomalies occur in 50-80% of individuals and may include renal agenesis, horseshoe kidney, or hydronephrosis.
Limb Abnormalities[edit]
Limb abnormalities are present in 40-50% of cases. These may include radial aplasia, polydactyly, or syndactyly.
Diagnosis[edit]
Diagnosis of VACTERL association is primarily clinical, based on the presence of at least three of the characteristic anomalies. Prenatal diagnosis may be possible through ultrasound and other imaging techniques, but many cases are identified after birth.
Management[edit]
Management of VACTERL association is multidisciplinary, involving pediatricians, surgeons, cardiologists, and other specialists. Treatment is tailored to the specific anomalies present in each individual and may include surgical correction of defects, supportive care, and ongoing monitoring for complications.
Prognosis[edit]
The prognosis for individuals with VACTERL association varies depending on the severity and combination of anomalies. With appropriate medical and surgical management, many individuals can lead healthy lives, although they may require ongoing medical care.
